104796-24-9

Usage

InChI:InChI=1/C12H14O6/c1-15-9-6-4-5-8(12(14)17-3)11(9)18-7-10(13)16-2/h4-6H,7H2,1-3H3

Upstream product

• 6342-70-7 3-methoxymethylsalicylate 
• 96-34-4 methyl chloroacetate 
• 96-32-2 bromoacetic acid methyl ester 

Downstream Products

• 863911-72-2 {2-(tetrahydropyran-2-yloxymethyl)-3-[2-(2,2,2-trifluoro-1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 863911-71-1 [3-[2-(1,1-diphenylbutylsulfanyl)ethyl]-2-(tetrahydropyran-2-yloxymethyl)benzofuran-7-yloxy]acetic acid methyl ester 
• 863911-70-0 [3-[2-(1,1-diphenylpropylsulfanyl)ethyl]-2-(tetrahydropyran-2-yloxymethyl)benzofuran-7-yloxy]acetic acid methyl ester 
• 863911-69-7 [3-[2-(1,1-diphenylethylsulfanyl)ethyl]-2-(tetrahydropyran-2-yloxymethyl)benzofuran-7-yloxy]acetic acid methyl ester 
• 863911-68-6 [3-(2-benzhydrylsulfanylethyl)-2-(tetrahydropyran-2-yloxymethyl)benzofuran-7-yloxy]acetic acid methyl ester 
• 863911-81-3 {2-(3-acetoxypropyl)-3-[2-(1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 863911-76-6 {2-hydroxymethyl-3-[2-(2,2,2-trifluoro-1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 863911-78-8 {2-(2-acetoxyethyl)-3-[2-(1,1-diphenylethylsulfanyl)ethyl]benzofuran-7-yloxy}acetic acid methyl ester 
• 863911-75-5 [3-[2-(1,1-diphenylbutylsulfanyl)ethyl]-2-hydroxymethylbenzofuran-7-yloxy]acetic acid methyl ester 
• 863911-74-4 [3-[2-(1,1-diphenylpropylsulfanyl)ethyl]-2-hydroxymethylbenzofuran-7-yloxy]acetic acid methyl ester 
• 863911-77-7 2-[3-[2-(1,1-diphenylethylsulfonyl)ethyl]-2-hydroxymethylbenzofuran-7-yloxy]acetic acid methyl ester 
• 863911-41-5 {3-[2-(1,1-diphenyl-ethylsulfanyl)-ethyl]-2-hydroxymethyl-benzofuran-7-yloxy}-acetic acid 
• 863911-73-3 [3-[2-(1,1-diphenylethylsulfanyl)ethyl]-2-hydroxymethylbenzofuran-7-yloxy]acetic acid methyl ester 
• 181051-95-6 [3-(2-benzhydrylsulfanylethyl)-2-hydroxymethylbenzofuran-7-yloxy]acetic acid methyl ester 

Relevant academic research and scientific papers

A practical preparation of 7-methoxy-3(2H)-benzofuranone

A practical new synthesis suitable for large-scale production of 7-methoxy-3(2H)-benzofuranone by conversion of commercially available 2-hydroxy-3-methoxybenzoic acid to 7-methoxy-3-acetoxybenzofuran followed by hydrolysis is described.

Synthetic models related to methoxalen - CYP2A6 interactions. Dimethoxybenzofuran derivatives as potent and selective inhibitors of cyp2a6

The human CYP2A6 enzyme metabolizes several xenobiotics including nicotine, the addictive component in tobacco. Reduced activity of CYP2A6, either for genetic reasons or by administering inhibitors of CYP2A6, reduces tobacco smoking. The reported compound